Spectroscopy of molecules with unstable nuclei
Maximilien Brice/CERN
With electronic, vibrational, and rotational energy states to account for, conducting spectroscopy of molecules can get complicated (see, for example, Physics Today, October 2019, page 18
Garcia Ruiz, Berger, and colleagues produced on the order of a million radium nuclei per second by firing protons at a uranium carbide target; some of the newly formed Ra then reacted with tetrafluoromethane gas to form RaF+ ions, which were separated and neutralized to form molecular RaF. Next, the researchers exposed the molecules to laser pulses designed to home in on their excitation energies. To quickly cover a wide swath of frequencies in the visible and IR, the team used three broadband lasers that probed the molecules, reflected off a mirror, and then probed the molecules again from the opposite direction; the reflected pulse explored a different frequency range due to a Doppler shift in the frame of the speedy molecules. A higher-power laser ionized any excited RaF molecules into RaF+, which were deflected via electric field onto a particle detector. The technique yielded the energies of multiple ground-to-excited RaF transitions.
Although the radium isotopes in the study (mass numbers 223–26 and 228) have half-lives on the order of days or years, Garcia Ruiz, Berger, and colleagues say the technique should be effective for analyzing species with half-lives of less than a second. Next, the team plans to use narrower-band laser pulses to obtain more precise spectroscopic measurements of RaF. To translate those measurements into stringent tests of fundamental physics (see the article by Dave DeMille, Physics Today, December 2015, page 34
Spectroscopy of molecules with unstable nuclei could also prove useful for fields like astrochemistry. In 2018 researchers observed the spectral signature of radioactive 26AlF in the emissions of a nova
More about the authors
Andrew Grant, agrant@aip.org